Identification of novel ATP13A2 interactors and their role in α-synuclein misfolding and toxicity-Reference-Cited by-同舟云学术

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Identification of novel ATP13A2 interactors and their role in α-synuclein misfolding and toxicity

Published:2012-05-29 Issue:17 Volume:21 Page:3785-3794
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Usenovic Marija,Knight Adam L.,Ray Arpita,Wong Victoria,Brown Kevin R.,Caldwell Guy A.,Caldwell Kim A.,Stagljar Igor,Krainc Dimitri

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/21/17/3785/17256088/dds206.pdf

Reference53 articles.

1. Clarifying lysosomal storage diseases;Schultz;Trends Neurosci.,2011

2. Neurodegenerative lysosomal disorders: continuum from development to late age;Nixon;Autophagy,2008

3. The lysosome and neurodegenerative diseases;Zhang;Acta Biochim. Biophys. Sin. (Shanghai),2009

4. Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase;Ramirez;Nat. Genet.,2006

5. ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson disease;Di Fonzo;Neurology,2007

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